Bifid nose
Symptom Information:
Symptom ID: | HPO:0011803 | ||||||
Synonyms: |
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Quality: | |||||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the face(HPO:0000271) Abnormality of the nose(HPO:0000366) Abnormal nasal morphology(HPO:0005105) Midline defect of the nose(HPO:0004122) Bifid nose(HPO:0011803) MedDRA: |
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Database Frequency: | 12 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Acromelic frontonasal dysplasia | (Orphanet:1827) |
BIFID NOSE, AUTOSOMAL DOMINANT | (OMIM:109740) |
BIFID NOSE, AUTOSOMAL RECESSIVE | (OMIM:210400) |
BNAR syndrome | (Orphanet:217266) |
Bifid nose | (Orphanet:2695) |
FRONTOFACIONASAL DYSPLASIA | (OMIM:229400) |
Fronto-facio-nasal dysostosis | (Orphanet:1791) |
HYDROLETHALUS SYNDROME 1 | (OMIM:236680) |
Hydrolethalus | (Orphanet:2189) |
Hypertelorism-microtia-facial clefting syndrome | (Orphanet:2213) |
Neurofaciodigitorenal syndrome | (Orphanet:2673) |
Trigonocephaly - bifid nose - acral anomalies | (Orphanet:3368) |